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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-Pyridinecarboxaldehyde, 2,5-dichloro-

O=Cc1cc(Cl)ncc1Cl Request for Quotation
Chemical Name: 4-Pyridinecarboxaldehyde, 2,5-dichloro-
CAS Number: 102645-33-0
Product Number: AG00080L(AGN-PC-0KKP84)
Synonyms:
MDL No:
Molecular Formula: C6H3Cl2NO
Molecular Weight: 176.0001

Identification/Properties

Computed Properties
Molecular Weight:
175.996g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
174.959g/mol
Monoisotopic Mass:
174.959g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
131
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2,5-Dichloropyridine-4-carboxaldehyde is a key intermediate in chemical synthesis, commonly used for its versatile applications in organic chemistry. This compound serves as a valuable building block for the synthesis of various advanced chemical compounds due to its unique structural properties and reactivity.In chemical synthesis, 2,5-Dichloropyridine-4-carboxaldehyde is frequently employed as a precursor in the formation of complex heterocyclic compounds. Its chlorinated pyridine ring moiety provides a convenient site for further functionalization through substitution reactions, enabling the introduction of a wide range of substituents and functional groups. This flexibility makes it an essential reagent in the production of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, 2,5-Dichloropyridine-4-carboxaldehyde plays a crucial role in the development of novel materials and bioactive molecules. Its ability to undergo diverse chemical transformations under mild reaction conditions makes it a valuable tool for synthesizing structurally intricate molecules with specific properties and functions. Researchers and chemists often rely on this compound to access new chemical structures and explore their potential applications in various fields.Overall, the versatility and reactivity of 2,5-Dichloropyridine-4-carboxaldehyde make it a indispensable reagent in the realm of chemical synthesis, enabling the efficient construction of complex organic molecules and facilitating the discovery of innovative compounds with diverse functionalities.